System, Test, Her-2/Neu, Ihc

FDA Pre-Market Approval

FDA Class 3 ·PATHWAY HER-2/NEU (4B5) RABBIT MONOCLONAL PRIMARY ANTIBODY

VG FEM BOX PROTECTOR

FDA UDI

Zimmer, Inc.·00889024589056·

ANTEGRADE FEM WORKING CHANNEL

FDA UDI

Biomet Orthopedics, LLC·00887868094279·

VG FEM BOX PROTECTOR

FDA UDI

Zimmer, Inc.·00889024589063·

ANTEGRADE FEM CONNECTING BOLT

FDA UDI

Biomet Orthopedics, LLC·00887868094835·

VG FEM BOX PROTECTOR

FDA UDI

Zimmer, Inc.·00889024589049·

ANTEGRADE FEM ENTRY TROCAR

FDA UDI

Biomet Orthopedics, LLC·05019279364565·

Adj Cutb - Fem Base

FDA UDI

Brainlab AG·04056481001827·

Salivary Estriol Test

FDA Pre-Market Approval

FDA Class 3 ·SALEST TM SYSTEM

DynaMesh-POSTERIOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

DYNAMESH-PP STANDARD, MODEL PP02NNNN, DYNAMESH-PP LIGHT, MODEL PP01NNNN

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

DynaMesh-VENTRAL

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

DYNAMESH -CICAT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Free estriol(FE3) Detection Kit(CLIA)

Device

EU IVDD · Eu Ivd General ·Shenzhen Zijian Biotechnology Co., Ltd·On the market

Iron Reagent (FE 2 x 200)

Device

EU IVDD · Eu Ivd General ·Beckman Coulter Inc.·On the market·32 countries

Reed Krakoff

FDA registration

Luxottica Mexico S.A. de C.V.·1 product·🇲🇽 Mexico

Burberry

FDA registration

Luxottica Mexico S.A. de C.V.·1 product·🇲🇽 Mexico

ACUMASTER BRAND ACUPUNCTURE NEEDLE

FDA 510(k)

FDA Class 2 ·General Hospital

TD-7301 Spirometer (TD-7301)

FDA 510(k)

FDA Class 2 ·Anesthesiology

PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY)

FDA 510(k)

FDA Class 1 ·General Hospital